NS-1209
CAS No. 245063-59-6
NS-1209( NS1209 | SPD502 )
Catalog No. M13710 CAS No. 245063-59-6
A selective, water-soluble, in vivo long-lasting AMPA antagonist with Ki of 43 nM; display selectivity for the [3H] AMPA over the [3H]kainate- (IC50=81 uM), [3H]CGS19755, and [3H]glycine-binding sites (IC50 > 30 uM) in rat cortical membranes.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
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Biological Information
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Product NameNS-1209
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NoteResearch use only, not for human use.
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Brief DescriptionA selective, water-soluble, in vivo long-lasting AMPA antagonist with Ki of 43 nM; display selectivity for the [3H] AMPA over the [3H]kainate- (IC50=81 uM), [3H]CGS19755, and [3H]glycine-binding sites (IC50 > 30 uM) in rat cortical membranes.
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DescriptionA selective, water-soluble, in vivo long-lasting AMPA antagonist with Ki of 43 nM; display selectivity for the [3H] AMPA over the [3H]kainate- (IC50=81 uM), [3H]CGS19755, and [3H]glycine-binding sites (IC50 > 30 uM) in rat cortical membranes; inhibits AMPA-induced currents in cortical neurons with IC50 of 0.15 uM; blocks AMPA-evoked spike activity in rat hippocampus (ED50=6.1mg/kg).Stroke Phase 2 Discontinued
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In Vitro——
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In Vivo——
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SynonymsNS1209 | SPD502
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PathwayMembrane Transporter/Ion Channel
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TargetiGluR
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RecptoriGluR
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Research AreaNeurological Disease
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IndicationStroke
Chemical Information
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CAS Number245063-59-6
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Formula Weight516.57
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Molecular FormulaC24H28N4O7S
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Purity>98% (HPLC)
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Solubility——
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SMILESO=C(O)[C@H](O/N=C1C2=C(C(C3)=C(CCN3C)C(C4=CC=C(C=C4)S(N(C)C)(=O)=O)=C2)NC/1=O)CCO
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Chemical Name(R,Z)-2-(((5-(4-(N,N-dimethylsulfamoyl)phenyl)-8-methyl-2-oxo-1,2,6,7,8,9-hexahydro-3H-pyrrolo[3,2-h]isoquinolin-3-ylidene)amino)oxy)-4-hydroxybutanoic acid
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Nielsen EO, et al. J Pharmacol Exp Ther. 1999 Jun;289(3):1492-501.
2. Erichsen HK, et al. Pain. 2002 Jul;98(1-2):151-61.
3. Langer M, et al. Neuropharmacology. 2011 Oct-Nov;61(5-6):1033-47.
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NS-1209
A selective, water-soluble, in vivo long-lasting AMPA antagonist with Ki of 43 nM; display selectivity for the [3H] AMPA over the [3H]kainate- (IC50=81 uM), [3H]CGS19755, and [3H]glycine-binding sites (IC50 > 30 uM) in rat cortical membranes.
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